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rs1023835002

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1023835002(A;G)
Make rs1023835002(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position44711547
GeneB2M, LOC102724979, PATL2
is asnp
is mentioned by
dbSNPrs1023835002
dbSNP (old)rs1023835002
ClinGenrs1023835002
ebirs1023835002
HLIrs1023835002
Exacrs1023835002
Gnomadrs1023835002
Varsomers1023835002
Maprs1023835002
PheGenIrs1023835002
Biobankrs1023835002
1000 genomesrs1023835002
hgdprs1023835002
ensemblrs1023835002
gopubmedrs1023835002
geneviewrs1023835002
scholarrs1023835002
googlers1023835002
pharmgkbrs1023835002
gwascentralrs1023835002
openSNPrs1023835002
23andMers1023835002
23andMe allrs1023835002
SNPshotrs1023835002
SNPdbers1023835002
MSV3drs1023835002
GWAS Ctlgrs1023835002
Max Magnitude0
ClinVar
Risk rs1023835002(G;G)
Alt rs1023835002(G;G)
Reference Rs1023835002(A;A)
Significance Probable-Pathogenic
Disease Multiple myeloma Adenocarcinoma of lung Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Colorectal Neoplasms Malignant lymphoma Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the head and neck Small cell lung cancer
Variation info
Gene B2M
CLNDBN Multiple myeloma Adenocarcinoma of lung Ovarian Serous Cystadenocarcinoma Adenocarcinoma of stomach Colorectal Neoplasms Malignant lymphoma, non-Hodgkin Squamous cell carcinoma of lung Malignant melanoma of skin Squamous cell carcinoma of the head and neck Small cell lung cancer
Reversed 0
HGVS NC_000015.9:g.45003745A>G; NC_000015.9:g.45003745A>T
CLNSRC
CLNACC RCV000417544.1, RCV000419609.1, RCV000420829.1, RCV000424715.1, RCV000424903.1, RCV000430542.1, RCV000435632.1, RCV000438049.1, RCV000441263.1, RCV000445210.1, RCV000421861.1, RCV000422880.1, RCV000425118.1, RCV000430300.1, RCV000431428.1, RCV000432545.1, RCV000432685.1, RCV000439880.1, RCV000440097.1, RCV000441906.1,